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				<datestamp>2013-06-30T03:41:05Z</datestamp>
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	<dc:title xml:lang="en-US">Regioselective synthesis of some functionalized 3,4’-bis-(pyrazolyl)ketones and chemoselectivity in their reaction with hydrazine hydrate</dc:title>
	<dc:creator>Hassaneen, Hamdi Mahmoud</dc:creator>
	<dc:creator>Shawali, Ahmad Sami</dc:creator>
	<dc:subject xml:lang="en-US">Enaminones</dc:subject>
	<dc:subject xml:lang="en-US">Enamino esters</dc:subject>
	<dc:subject xml:lang="en-US">Regioselectivity</dc:subject>
	<dc:subject xml:lang="en-US">Chemoselectivity</dc:subject>
	<dc:subject xml:lang="en-US">Hydrazonoyl halides</dc:subject>
	<dc:subject xml:lang="en-US">Pyrazolo[3</dc:subject>
	<dc:subject xml:lang="en-US">4-d]pyridazines</dc:subject>
	<dc:description xml:lang="en-US">A new enamino ester, (E)-ethyl 3-(dipropylamino)acrylate, was prepared and used for synthesis of various pyrazole derivatives, 4a-k and 5a-d. Other new enaminone, (E)-ethyl 3-(3-(dimethylamino)acryloyl)-1-(4-nitrophenyl)-1H-pyrazole-4-carboxylate (8), was also prepared from compound 4a and utilized as precursor for synthesis of different functionalized 3,4&#039;-bis-pyrazolyl ketones 9a-c, 10a-c. The site selectivity in hydrazinolysis of the latter was studied. The structures of the products namely pyrazolo[3,4-d]pyridazine derivatives 11(13) were confirmed by spectral and elemental analyses and by alternate unambiguous synthesis.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2013-06-30</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/723</dc:identifier>
	<dc:identifier>10.5155/eurjchem.4.2.102-109.723</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 4 No. 2 (2013): June 2013; 102-109</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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